Clinical Trial Site Liaison
We're partnering with a clinical-stage biopharmaceutical company seeking an experienced Clinical Trial Site Liaison to support clinical research activities across Italy. This is a hands‑on contract role focused on building relationships with investigators and clinical trial sites, supporting study delivery, and working closely with Clinical Operations teams and CRO partners. Candidates with a background in clinical operations, site management or clinical trial liaison roles are encouraged to connect. Scorra verso il basso per trovare i dettagli completi dell'offerta, inclusa l'esperienza richiesta e le mansioni associate.
* Experience as a CTSL/CTL, CRA, CTM, Clinical Project Manager or similar.
* Strong clinical trial and investigator‑site experience.
* MSL experience considered, ideally alongside clinical trial exposure.
* GCP knowledge and experience working with investigators, sites and CROs.
* Experience with autoimmune, neurology or neuroscience backgrounds.
* Fluent Italian and based in Italy. Professional Traits & Work Ethic Strong communication and relationship‑building skills. Proactive, organised and reliable, with a service‑oriented approach. Comfortable working independently within an international team. Willing to travel nationally across Italy. Role Responsibilities
* Build relationships with investigators and clinical research sites.
* Support site engagement, study start‑up and ongoing trial delivery.
* Liaise between the sponsor, CRO and internal clinical teams.
* Address site needs and support GCP‑compliant study conduct. Contract: Initial 12 months, with potential extension. Commitment: Full-time preferred; 0.5–0.8 FTE considered. xlwpduy
Location:
Home-based in Italy, with national travel occasionally. #J-18808-Ljbffr
* Experience as a CTSL/CTL, CRA, CTM, Clinical Project Manager or similar.
* Strong clinical trial and investigator‑site experience.
* MSL experience considered, ideally alongside clinical trial exposure.
* GCP knowledge and experience working with investigators, sites and CROs.
* Experience with autoimmune, neurology or neuroscience backgrounds.
* Fluent Italian and based in Italy. Professional Traits & Work Ethic Strong communication and relationship‑building skills. Proactive, organised and reliable, with a service‑oriented approach. Comfortable working independently within an international team. Willing to travel nationally across Italy. Role Responsibilities
* Build relationships with investigators and clinical research sites.
* Support site engagement, study start‑up and ongoing trial delivery.
* Liaise between the sponsor, CRO and internal clinical teams.
* Address site needs and support GCP‑compliant study conduct. Contract: Initial 12 months, with potential extension. Commitment: Full-time preferred; 0.5–0.8 FTE considered. xlwpduy
Location:
Home-based in Italy, with national travel occasionally. #J-18808-Ljbffr